Extended Data Fig. 6: The effect of BAR deficiency on Treg cells or TH17 cells in gut and peripheral lymphoid organs.
From: Microbial bile acid metabolites modulate gut RORγ+ regulatory T cell homeostasis

a, Protein expression of VDR, FXR (also known as NR1H4) and GPBAR1 in the colonic tissue of SPF C57BL/6J mice was analysed by western blot. The red asterisks indicate the corresponding molecular weight of VDR (53 kDa), FXR (69 kDa) and GPBAR1 (33 kDa). For gel source data, see Supplementary Fig. 1. b, c, Absolute numbers of RORγ+Heliosā in the colonic FOXP3+CD4+TCRβ+Ā Treg cell population (b) and of FOXP3+Ā Treg cells in the CD4+TCRβ+ population (c) from mice deficient in nuclear receptors (Nr1i2ā/āNr1i3ā/ā, Nr1h3ā/ā, Vdrā/ā, Nr1h4ā/ā and Vdrā/āNr1h4ā/ā) and their littermate controls. d, e, Frequencies of FOXP3+ in the colonicĀ CD4+TCRβ+ cell population from mice deficient in G-protein-coupled receptors (Gpbar1ā/ā, Chrm2ā/ā, Chrm3ā/ā and S1pr2ā/ā) and their littermate controls (d) and from mice deficient in nuclear receptors (Nr1i2ā/āNr1i3ā/ā, Nr1h3ā/ā, Vdrā/ā, Nr1h4ā/ā and Vdrā/āNr1h4ā/ā) and their littermate controls (e). f, g, Frequencies of RORγ+FOXP3ā in the colonicĀ CD4+TCRβ+ cell population from mice described in d and e. hān, Treg cells in the spleen, mesenteric lymph node and ileum from the indicated mice were analysed. Frequencies of RORγ+Heliosā in the FOXP3+CD4+TCRβ+Ā Treg cell population from Gpbar1ā/ā (h), Chrm2ā/ā (i), Chrm3ā/ā (j), S1pr2ā/ā (k), Nr1i2ā/āNr1i3ā/ā (l), Nr1h3ā/ā (m), and Vdrā/ā, Nr1h4ā/ā and Vdrā/āNr1h4ā/ā (n) mice and their littermate controls are shown. Data are representative of two or three independent experiments in a and dān, or are pooled from two or three independent experiments in b and c. n represents biologically independent animals. Data are mean ± s.e.m. **PĀ <Ā 0.01, one-way ANOVA followed by the Bonferroni postĀ hoc test.